A spacer system replaces or substitutes for a medical implant in a patient. The system includes a housing comprising a shape similar to the medical implant; an aperture in the housing, a subcutaneous port configured to receive a medicament, the subcutaneous port being in fluid communication with the aperture; and at least one channel within the housing, wherein the at least one channel extends from the aperture to an exterior surface of the housing to equally distribute a material the medicament from the aperture through the at least one channel. The subcutaneous port is in fluid communication with the aperture through a catheter connecting the subcutaneous port to the aperture. The system may be used to replace a variety of medical implants, including a hip implant, an intramedullary nail, a pedicle screw, a knee implant, a sternum prosthesis, and a clavicle prosthesis, an ankle implant, shoulder implant, tibia implant, femur implant, humerus implant, spinal cage, external fixation pin, intercalary fusion device, talus implant, or a vertebral body implant.

A proposed treatment of arthrosis/osteoarthritis in a joint of a mammal or human patient involves deposing a liquid material on at least one damaged surface of the joint. To accomplish this, a reservoir (110) is provided, which holds a volume of a biocompatible material in liquid form outside of a body containing the joint (J) to be treated. A proximal end (P) of a tub e-shaped instrument (120) is connected to the reservoir (110), and a distal end (D) of the instrument (120) is inserted into the joint (J). The liquid material is fed through the instrument (120) to the distal end (D) for deposition on the at least one damaged joint surface.

The material is configured to assume a solid form under predefined conditions (e.g. when cooling off, or being exposed to a specific type of radiation). When the material has the solid form, it has a resistance to wear adapted to replace a worn out joint surface.

A lubrication device for lubricating a joint of a human or mammal patient, which is entirely implantable in a patient's body, comprises a reservoir for storing a lubricating fluid and a fluid connection for introducing the lubricating fluid into the joint when the device is implanted in the patient's body. Further, the fluid connection comprises a fluid connection device connecting the reservoir with the joint such that a lubricating fluid flow is established from the reservoir into the joint. The fluid connection comprises either an infusion needle adapted to be intermittently placed into the joint for injecting the lubricating fluid, or a tube adapted to be permanently placed into the joint for continuously injecting the lubricating fluid.

This invention comprises a novel approach for the refixation of a loosened implant to bone, wherein the novel approach comprises providing access to a boundary region between the implant and the bone; removing abnormal interface tissue, wear debris and/or bone cement debris from the boundary region; and inserting bone fixation material into the boundary region so that the bone fixation material engages the implant and the bone and thereby effects refixation of the loosened implant to the bone.

A modular spacer device implantable in the human body for the treatment of an infected articular seat includes a stem element, a head or ball element and coupling elements between the stem element and the head, wherein such coupling elements comprise a plurality of elongated teeth, placed at pre-established distances from each other, and a plurality of housing seats for the teeth.

A temporary spacer device for a joint of the human body such as a knee joint includes a first component or femoral component, adapted to be constrained to a bone or to the femoral bone of a patient, at the joint of the human body; a second component or tibial component, adapted to be constrained to a bone or tibial bone of a patient, at the joint of the human body, and at least one stem having a proximal end, wherein the first component or femoral component and/or the second component or tibial component include at least one housing seat for the proximal end of the at least one stem, adapted to allow the inclination and/or rotation of the at least a stem with respect to an insertion axis of the proximal end into the at least one housing seat.

Disclosed herein is a temporary knee spacer system for the temporary replacement of a knee joint, which is designed for the interim phase of two-stage septic revisions of knee joint total endoprostheses. The knee spacer system can be used in particular with two-phase septic revisions with which two or more microbial germs are the cause of an infection of the knee joint total endoprosthesis and the surrounding tissue.

An acetabular spacer device, of a type that is temporary and disposable, adapted to be implanted in use in a bone cavity placed at a joint of the human body, such as a hip or shoulder joint, has a cup-like shape, substantially hemispherical, and includes a first convex surface, adapted to be positioned at the bone cavity, a second concave surface, which defines a cavity, further includes at least one pharmaceutical or medical substance, such as at least one antibiotic, adapted to treat during use an ongoing infection in the bone cavity.

Provided for herein, in several embodiments are implants and methods of using same to repair damaged or defective soft tissue. In several embodiments, the soft tissue comprises cartilage within a joint space. In several embodiments, the implants provided for comprise a stimulating region and an anchoring region. In several embodiments, the implants are spherical. A discontinuity between a surface of the implant and the surrounding cartilage advantageously facilitates implant placement and stimulation of generation of fibrous tissue, and subsequently new cartilage.

A system for implanting an inter-body device between adjacent vertebrae comprises an inter-body device having a plurality of cans secured to a flexible bridge and having a relief portion therebetween. An inserter tube and complementary bullnoses are advantageously secured to the vertebrae by an extension arm for securing the assembly precisely in place. A plurality of articulating trial implants are provided to test fit a disc space for the proper sized inter-body device.